High carbon iron filings (HCIF) and metal reducing bacteria (Serratia sp.) co-assisted Cr (VI) reduction: Kinetics, mechanism and longevity

2019 ◽  
Vol 236 ◽  
pp. 388-395 ◽  
Author(s):  
Shivangi Upadhyay ◽  
Amal Krishna Saha ◽  
Alok Sinha
2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Shivangi Upadhyay ◽  
Alok Sinha

AbstractIn this study, a bacterial strain Serratia sp. was employed for the reduction of synthetically prepared different concentration of Cr(VI) solution (10, 25, 40, 50 and 100 mg/L). Cometabolism study have been carried out in the binary substrate system as well as in the tertiary substrate system. The results revealed that when glucose was added as a co-substrate, at low Cr(VI) concentration, complete reduction was achieved followed by increased biomass growth, but when Cr(VI) concentration was increased to 100 mg/L, the reduction decline to 93%. But in presence of high carbon iron filings (HCIF) as co-substrate even at higher Cr(VI) concentration i.e. 100 mg/L, 100% reduction was achieved and the cell growth continued till 124 h. The study was illustrated via Monod growth kinetic model for tertiary substrate system and the kinetic parameters revealed that the HCIF and glucose combination showed least inhibition to hexavalent chromium reduction by Serratia sp.


2002 ◽  
Vol 80 (6) ◽  
pp. 637-649 ◽  
Author(s):  
Chongxuan Liu ◽  
Yuri A. Gorby ◽  
John M. Zachara ◽  
Jim K. Fredrickson ◽  
Christopher F. Brown

Alloy Digest ◽  
1970 ◽  
Vol 19 (7) ◽  

Abstract INCOLOY ALLOY 802 is a high-carbon iron-base alloy recommended for high-temperature applications requiring excellent corrosion resistance and good mechanical properties. It is furnished in the annealed condition. This datasheet provides information on composition, physical properties, hardness, elasticity, and tensile properties as well as fracture toughness, creep, and fatigue. It also includes information on high temperature performance and corrosion resistance as well as forming, heat treating, machining, and joining. Filing Code: SS-240. Producer or source: Huntington Alloy Products Division, An INCO Company.


2011 ◽  
Vol 45 (3) ◽  
pp. 951-957 ◽  
Author(s):  
Andrew E. Plymale ◽  
James K. Fredrickson ◽  
John M. Zachara ◽  
Alice C. Dohnalkova ◽  
Steve M. Heald ◽  
...  

2018 ◽  
Vol 84 (20) ◽  
Author(s):  
Lulu Liu ◽  
Shisheng Li ◽  
Sijing Wang ◽  
Ziyang Dong ◽  
Haichun Gao

ABSTRACT Shewanella oneidensis is an extensively studied bacterium capable of respiring minerals, including a variety of iron ores, as terminal electron acceptors (EAs). Although iron plays an essential and special role in iron respiration of S. oneidensis, little has been done to date to investigate the characteristics of iron transport in this bacterium. In this study, we found that all proteins encoded by the pub-putA-putB cluster for putrebactin (S. oneidensis native siderophore) synthesis (PubABC), recognition-transport of Fe3+-putrebactin across the outer membrane (PutA), and reduction of ferric putrebactin (PutB) are essential to putrebactin-mediated iron uptake. Although homologs of PutA are many, none can function as its replacement, but some are able to work with other bacterial siderophores. We then showed that Fe2+-specific Feo is the other primary iron uptake system, based on the synthetical lethal phenotype resulting from the loss of both iron uptake routes. The role of the Feo system in iron uptake appears to be more critical, as growth is significantly impaired by the absence of the system but not of putrebactin. Furthermore, we demonstrate that hydroxyl acids, especially α-types such as lactate, promote iron uptake in a Feo-dependent manner. Overall, our findings underscore the importance of the ferrous iron uptake system in metal-reducing bacteria, providing an insight into iron homeostasis by linking these two biological processes. IMPORTANCE S. oneidensis is among the first- and the best-studied metal-reducing bacteria, with great potential in bioremediation and biotechnology. However, many questions regarding mechanisms closely associated with those applications, such as iron homeostasis, including iron uptake, export, and regulation, remain to be addressed. Here we show that Feo is a primary player in iron uptake in addition to the siderophore-dependent route. The investigation also resolved a few puzzles regarding the unexpected phenotypes of the putA mutant and lactate-dependent iron uptake. By elucidating the physiological roles of these two important iron uptake systems, this work revealed the breadth of the impacts of iron uptake systems on the biological processes.


1991 ◽  
Vol 22 (1) ◽  
pp. 251-253 ◽  
Author(s):  
H. Era ◽  
K. Kishitake ◽  
F. Otsubo ◽  
E. Tanaka

2016 ◽  
Vol 74 (5) ◽  
pp. 1217-1226
Author(s):  
Raja Kumar ◽  
Alok Sinha

This study proposed that the physicochemical effects of common dyebath auxiliaries on the bulk dye solution as well as on the iron surface can influence the reductive discoloration of effluent containing Acid Orange 7 (AO7) dye using high-carbon iron filings. Sodium chloride increased the discoloration rate because of the pitting corrosion on the iron surface, triggered by chloride anion. ‘Salting out’ effect of ammonium sulfate improved the reaction rate up to a certain concentration, beyond which it could compete with dye molecules for the reactive sites, as revealed by formed sulfite and sulfide. Urea drastically reduced the discoloration rates by its chaotropic effect on the bulk solution and by wrapping around the iron surface. Organic acids, namely acetic acid and citric acid, stimulated iron corrosion to improve the discoloration rates. The discoloration reaction was biphasic with an initial fast reaction phase, where in every case more than 70% discoloration was observed within 5 min of reaction, preceding a slow reaction phase. The experimental data could be well described using biphasic kinetics equation (R2> 0.997 in all cases) and a biphasic equation was developed considering the individual impact of co-existing auxiliaries on AO7 discoloration.


1999 ◽  
Vol 85 (9) ◽  
pp. 639-644 ◽  
Author(s):  
Etsurou SHIBATA ◽  
Takashi SATO ◽  
Katsumi MORI
Keyword(s):  

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